ID   GM20398
AC   CVCL_U304
DR   CLO; CLO_0029569
DR   Coriell; GM20398
DR   Wikidata; Q54851006
CC   Sequence variation: Mutation; HGNC; HGNC:5157; HPRT1; Simple; p.Asp194His (c.580G>C); ClinVar=VCV000284173; Zygosity=Hemizygous (Coriell=GM20398).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C61255; Lesch-Nyhan syndrome
DI   ORDO; Orphanet_510; Lesch-Nyhan syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   Age unspecified
CA   Finite cell line
DT   Created: 03-02-14; Last updated: 19-12-24; Version: 15
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